240136-69-0 Usage
General Description
2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE is a chemical compound with the molecular formula C9H7N5O2. It is a pyrimidine derivative with an amino group and a nitrophenyl group attached to the pyrimidine ring. 2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE has potential applications in pharmaceutical and agrochemical industries due to its biological activities, such as anti-inflammatory and anti-cancer properties. It can also serve as an intermediate in the synthesis of various organic compounds. Additionally, the nitrophenyl group in 2-AMINO-4-(3-NITROPHENYL)PYRIMIDINE allows for easy functionalization, making it an attractive target for chemical modification and further development of new compounds with enhanced properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 240136-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,1,3 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 240136-69:
(8*2)+(7*4)+(6*0)+(5*1)+(4*3)+(3*6)+(2*6)+(1*9)=100
100 % 10 = 0
So 240136-69-0 is a valid CAS Registry Number.
240136-69-0Relevant articles and documents
COMPOUNDS
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Page/Page column 56, (2017/03/14)
A compound of Formula (I), or a salt thereof, compositions comprising the compound, processes for its preparation and its use in therapy, for example in the treatment of parasitic diseases such as Chagas disease, Human African Trypanosomiasis (HAT), Anima
Assessment of new triplet forming artificial nucleobases as RNA ligands directed towards HCV IRES IIId loop
Safir Filho, Mauro,Martin, Anthony R.,Benhida, Rachid
, p. 1780 - 1783 (2017/04/03)
We report the synthesis of two new artificial nucleobase scaffolds, 1 and 2, featuring adequate hydrogen bonding donors and acceptors for the molecular recognition of U:A and C:G base pairs, respectively. The tethering of these structures to various amino acids and the assessment of these artificial nucleobase-amino acid conjugates as RNA ligands against a model of HCV IRES IIId domain are also reported. Compound 1e displayed the highest affinity (Kd twice lower than neomycin – control). Moreover, it appears that this interaction is enthalpically and entropically favored.
